Relevant bibliographies by topics / 1-amino-2- naphthole

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Academic literature on the topic '1-amino-2- naphthole'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "1-amino-2- naphthole"

1

Maringgele, Walter, and Anton Meller. "Reaktionen der Natrium-Komplexe aromatischer Ether mit Dichlor(diorganylamino)boranen/Reactions of Sodium Complexes of Aromatic Ethers with Dichloro(diorganylamino)boranes." Zeitschrift für Naturforschung B 44, no. 1 (1989): 67–73. http://dx.doi.org/10.1515/znb-1989-0116.

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Abstract The reaction of anisole with Na/K-alloy and subsequent reaction with dichloro(diisopropyl-amino)borane yields diisopropylamino(diphenoxy)borane (1). In reacting the sodium complex of 1-or 2-m ethoxynaphthalene, respectively, with dichloro(diorganylamino)boranes the ether bond is cleaved. One obtains the methoxy-2-naphthoxy-diorganylam inoboranes (2a -d) besides the di-2-naphthoxy-diorganylam inoboranes (3a-e), the 2-naphthoxy-bis(diorganylamino)boranes (4a-b) and the solvated sodium-2-naphtholate (6). By-products are 1,2-bis[(diisopropylamino)-1- or 2-naphthoxyboryl]ethyne derivatives
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2

El-Naggar, Mohamed, Abdel-Nasser El-Shorbagi, Dina H. Elnaggar, Abd El-Galil E. Amr, Mohamed A. Al-Omar, and Elsayed A. Elsayed. "Synthesis, Characterization, and Cytotoxic Evaluation of Some Newly Substituted Diazene Candidates." Journal of Chemistry 2018 (November 1, 2018): 1–9. http://dx.doi.org/10.1155/2018/3626824.

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A series of azocompounds containing methyl salicylate 4a–k and 1-naphthyl moiety 6–8 was synthesized and tested as anticancer agents. Nitrosation of methyl 5-amino-2-hydroxybenzoate or 1-aminonaphthalene by using NaNO2 in the presence of HCl afforded diazonium salt derivatives 2 and 5, which were treated with substituted imino or substituted amino derivatives, to give the corresponding substituted amino-pent-2-en-3-yl-diazenylbenzoate 4a–k or 2-substituted-1-(naphthalen-1-yl)diazene derivatives 6a–h, 7a,b, and 8a,b. All the synthesized compounds were elucidated by elemental analysis and spectr
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3

Ibrahim, Mohamed N., Salaheddin A. I. Sharif, Ahmad N. EL-Tajory, and Asma A. Elamari. "Synthesis and Antibacterial Activities of Some Schiff Bases." E-Journal of Chemistry 8, no. 1 (2011): 212–16. http://dx.doi.org/10.1155/2011/258340.

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Schiff basesp-hydroxybenzylidene-2-carboxyaniline,p-nitrobenz-ylidene-2-carboxyaniline,p-(N, N-dimethyl)aminobenzylidene-2-carboxyaniline,N-(4-hydroxybezylidene)-benzene-1,2-diamine,N--(4-nitrobezylidene)benzene-1,2-diamine,N-(4-(N, N-dimethylaminobezylidene)benzene-1,2-diamine,N-(4-(N,N-dimethylamino)benzylidene)naphthalen-1-amine,N-(4-nitrobenzylidene)naphthalen-1-amine,N--(4-chlorobenzylidene)naphthalen-1-amine,sodium-4-(4-(N,N-dimethyl amino)benzylideneamino)naphthalene-1-sulfonate,sodium -4-(4-nitrobenzylidene-amino)naphthalene-1-sulfonate and sodium-4-(4-chlorobenzylideneamino) naphthale
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4

Dilip, Kumar, Vaish Anurag, and Nayan Ram. "Equilibrium studies on binary and ternary complexes of palladium and cadmium with some nitrogen and oxygen donor ligands." Journal of Indian Chemical Society Vol. 82, Jun 2005 (2005): 490–93. https://doi.org/10.5281/zenodo.5830426.

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Department of Chemistry, Hindu College, Moradabad-244 001, India <em>E-mail</em>: ramnayan_2003@yahoo.co.in&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; Fax: 91-591-2440070 <em>Manuscript received 26 August 2003, revised 9 November 2004, accepted 2 March 2005</em> The metal-ligand equilibrium reactions involving palladium(II), cadmium(ll) and 1,2-dihydroxybenzene, 1-amino-2-naphthol4-sulfonic acid, 8-amino-1-naphthol-3,6-disulfonic acid, <em>o</em>-aminophenol and 4,5-dihydroxybcnzene-1 ,3-disulfonic acid have been studied in solution at 25&ordm; and at ionic strength of 0.10 <em>M</em> (KNO<sub>3</sub>)
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5

Journal, Baghdad Science. "Preparation of some azo compounds by diazotization and coupling of 2- amino -5 – thiol -1,3,4- thiadizaole." Baghdad Science Journal 4, no. 2 (2015): 271–75. http://dx.doi.org/10.21123/bsj.4.2.271-275.

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2- amino -5- thiol-1,3,4- thiadiazole (S1) was prepared by cyclic locking of thiosemicarbazide in the presence of anhydrous sodium carbonate and CS2. diazotization of (S1) compound gave diazonium salt (S2) that reacts with different activated aromatic compounds to get the following azo compounds ,2 [(4- aminophenyl) diazenyl ] 1,3,4- thiazdiazole-5- thiol (S3) ,2-[4-amino- 1-naphthyl diazenyl] -1,3,4 – thiazdiazole-5-thiol (S4) , 3-amino-4-[(5- mercapto -1,3,4- thiadiazole -2-yl) diazenyl ] phenol(S5) ,1-[(5-mercapto-1,3,4-thiadiazole-2-yl) diazenyl] -2-naphthol (S6) , 5-{[4-(dimethylamino) ph
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Saleh, Mohammad M., and Suhair S. Dauood. "Preparation of some azo compounds by diazotization and coupling of 2- amino -5 – thiol -1,3,4- thiadizaole." Baghdad Science Journal 4, no. 2 (2021): 271–75. http://dx.doi.org/10.21123/bsj.2007.4.2.271-275.

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2- amino -5- thiol-1,3,4- thiadiazole (S1) was prepared by cyclic locking of thiosemicarbazide in the presence of anhydrous sodium carbonate and CS2. diazotization of (S1) compound gave diazonium salt (S2) that reacts with different activated aromatic compounds to get the following azo compounds ,2 [(4- aminophenyl) diazenyl ] 1,3,4- thiazdiazole-5- thiol (S3) ,2-[4-amino- 1-naphthyl diazenyl] -1,3,4 – thiazdiazole-5-thiol (S4) , 3-amino-4-[(5- mercapto -1,3,4- thiadiazole -2-yl) diazenyl ] phenol(S5) ,1-[(5-mercapto-1,3,4-thiadiazole-2-yl) diazenyl] -2-naphthol (S6) , 5-{[4-(dimethylamino) ph
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Xu, Ji-Jun, Jun Li, Min Pi, and Chuan-Ming Jin. "1-[(Phenyliminio)amino]-2-naphtholate." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1752. http://dx.doi.org/10.1107/s1600536810023329.

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8

Swetha, Vandana P., Aditya Basu, and Prashant S. Phale. "Purification and Characterization of 1-Naphthol-2-Hydroxylase from Carbaryl-Degrading Pseudomonas Strain C4." Journal of Bacteriology 189, no. 7 (2007): 2660–66. http://dx.doi.org/10.1128/jb.01418-06.

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ABSTRACT Pseudomonas sp. strain C4 metabolizes carbaryl (1-naphthyl-N-methylcarbamate) as the sole source of carbon and energy via 1-naphthol, 1,2-dihydroxynaphthalene, and gentisate. 1-Naphthol-2-hydroxylase (1-NH) was purified 9.1-fold to homogeneity from Pseudomonas sp. strain C4. Gel filtration and sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed that the enzyme is a homodimer with a native molecular mass of 130 kDa and a subunit molecular mass of 66 kDa. The enzyme was yellow, with absorption maxima at 274, 375, and 445 nm, indicating a flavoprotein. High-performance liqui
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9

Capozzi, Maria Annunziata M., and Cosimo Cardellicchio. "(S,S)-1-(Phenyl((1′-4-nitrophenyl-ethyl)amino)methyl)-2-naphthol." Molbank 2022, no. 4 (2022): M1522. http://dx.doi.org/10.3390/m1522.

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The Betti reaction of 2-naphthol, benzaldehyde and (S)-1-(4-nitrophenyl)ethylamine without any solvent gave the corresponding aminobenzylnaphthol, that is the (S,S)-1-(phenyl((1′-4-nitrophenyl-ethyl)amino)methyl)-2-naphthol, in good yield (56%). The absolute configuration of the title compound was attributed by NMR analysis, a procedure that is reliable if compared with the data obtained by X-ray diffraction experiments.
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El-Gaby, Mohamed S. A., Mohamed I. Hassan, Modather F. Hussein, Ahmed M. Ali, Mahmoud M. Elaasser, and Faraghally A. Faraghally. "Synthesis, characterization and in vitro biological screening of 4-hydroxy naphthalen-1-yl, naphtho[1,2-b]furan, benzo[h]chromene and 5,6-dihydropyridazine derivatives containing sulfonamide moiety." Mediterranean Journal of Chemistry 7, no. 5 (2018): 346–58. http://dx.doi.org/10.13171/mjc751912061355msaeg.

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In this study, a series of 4-((4-hydroxynaphthalen-1-yl)diazenyl)benzenesulfonamides have been prepared by subsequent diazotization of sulfonamide derivatives and coupling with 1-naphthol in alkaline medium. Cyclization of 4-((4-hydroxynaphthalen-1-yl)diazenyl)benzenesulfonamides with cinnamic acid in the presence of a basic catalyst afforded the novel naphtho[1,2-b]furans. Also, 4-((4-hydroxynaphthalen-1-yl)diazenyl)benzenesulfonamides can be cyclized with α‐cyanocinnamonitriles to afford 2-amino-3-cyano-4-phenyl-4H-benzo[h]chromenes. 4-(4-amino-3,5- dicyano-6-iminopyridazin-1(6H)-yl)benzenes
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Book chapters on the topic "1-amino-2- naphthole"

1

Winkelmann, Jochen. "Diffusion coefficient of 1-amino-2-naphthol in water." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_880.

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Winkelmann, Jochen. "Diffusion coefficient of 1-amino-2-naphthol-4-sulfonic acid in water." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_886.

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Shin Jonghan, Kepe Vladimir, Barrio Jorge R., and Small Gary W. "The Merits of FDDNP-PET Imaging in Alzheimer's Disease." In Advances in Alzheimer’s Disease. IOS Press, 2011. https://doi.org/10.3233/978-1-60750-793-2-265.

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2-(1-{6-[(2-[fluorine-18]fluoroethyl)(methyl)amino]-2-naphthyl}-ethylidene)malononitrile (FDDNP) is the first positron emission tomography (PET) molecular imaging probe to visualize Alzheimer's disease (AD) pathology in living humans. The most unique features of FDDNP are that (1) it is the only currently available radiotracer to image neurofibrillary tangles, beside amyloid aggregates, in living humans; and (2) it is also the only radiotracer to visualize AD pathology in the hippocampal region of living humans. In this article, we discuss FDDNP&amp;apos;s unique ability to image tau pathology
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4

Liao, C. C., and R. K. Peddinti. "Oxidation of 1-Amino-2-naphthol by Polymer-Supported Hypochlorite Ion." In Quinones and Heteroatom Analogues. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-028-00294.

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